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ABOUT THIS PAGE
A Macimorelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Macimorelin, including repackagers and relabelers. The FDA regulates Macimorelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Macimorelin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Macimorelin supplier is an individual or a company that provides Macimorelin active pharmaceutical ingredient (API) or Macimorelin finished formulations upon request. The Macimorelin suppliers may include Macimorelin API manufacturers, exporters, distributors and traders.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Macimorelin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Macimorelin API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Macimorelin as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Macimorelin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Macimorelin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Macimorelin suppliers with NDC on PharmaCompass.
Macimorelin Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Macimorelin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Macimorelin GMP manufacturer or Macimorelin GMP API supplier for your needs.
A Macimorelin CoA (Certificate of Analysis) is a formal document that attests to Macimorelin's compliance with Macimorelin specifications and serves as a tool for batch-level quality control.
Macimorelin CoA mostly includes findings from lab analyses of a specific batch. For each Macimorelin CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Macimorelin may be tested according to a variety of international standards, such as European Pharmacopoeia (Macimorelin EP), Macimorelin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Macimorelin USP).
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